BackgroundChildren's complex middle cerebral artery (MCA) aneurysm is a relatively rare occurrence. When the huge aneurysm is located in the MCA bifurcation with an inconspicuous neck and involving numerous arteries, intravascular interventional surgery or aneurysm clipping are often difficult treatment options. At this point, high flow bypass revascularization is necessary as a treatment to preserve cerebral blood flow. In recent years, the internal maxillary artery (IMA) has gradually become the mainstream donor artery of thw high flow bypass. We performed internal maxillary artery -radial artery-middle cerebral artery (IMA-RA-MCA) and superficial temporal artery-middle cerebral artery (STA-MCA) bypass as the treatment of a complex MCA bifurcation aneurysm in consideration of the patient's condition and the advantage of the IMA. According to the author, this case is the youngest reported case of IMA-RA-MCA bypass at present.Case DescriptionA male child, 7 years and 8 months, was admitted to the hospital due to “recurrent headache for more than 9 months,” DSA indicated that there was a large wide-necked aneurysm at the bifurcation of the right MCA M1 segment, with a size of about 1.16*1.58*1.32 cm. The inflow path of the aneurysm was in front of M1 bifurcation, and one outflow path originated from the aneurysm body, and another small outflow path attached to the aneurysm body. After completing the preoperative evaluation, an extended pterional approach with zygomatic osteotomy was performed to fully expose the aneurysm and IMA, harvesting the left radial artery at the same time, then a STA-MCA bypass, IMA-RA-MCA bypass, and aneurysm trapping were performed. postoperative re-examination showed that bypass vessels and the distal middle artery vessels were patent and the aneurysm disappeared, the child has no neurological dysfunction.ConclusionsIMA-RA-MCA bypass is an effective high-flow cerebral blood reconstruct scheme in the treatment of complex middle cerebral artery bifurcation aneurysms. This case can provide a reference for the surgical treatment of complex middle cerebral artery bifurcation aneurysms in children.

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Background By comparing the effectiveness of the double-barrel and single-branch STA-MCA bypass in treating moyamoya disease, investigate whether the double-barrel bypass is more advantageous. Methods An analysis of the clinical records of patients with moyamoya disease treated with surgery was conducted retrospectively and divided into two groups: double-barrel bypass and single-branch bypass. Preoperative and postoperative rates of intracerebral hemorrhage, cerebral infarction, epilepsy, transient neurological deficits (TNEs), and mRS score were compared. Comparing changes in cerebral computed tomography perfusion (CTP) values of surgical side MCA pre-operation, one week and six months postoperatively between the two groups or within the same group was also performed. Results A total of 48 patients were enrolled, including 22 in the double-barrel group and 26 in the single-branch group. Between the two groups, there were no significant differences in postoperative hemorrhage, cerebral infarction, epilepsy, TNEs, mRS scores 6 months postoperatively, or CTP values 6 months postoperatively. Compared with preoperative values, the cerebral perfusion value of two groups decreased one week after surgery, but it improved six months later. Conclusions Both STA-MCA bypass methods can effectively improve cerebral blood perfusion and achieve therapeutic goals. Double-barrel bypass does not increase the risk of perioperative cerebral hemorrhage, infarctions, epilepsies, or TNEs, but it does show no significant advantages over single-branch bypass. As one surgical option for some patients with moyamoya disease, we believe double-barrel bypass can be used, but its priority is not greater than single-branch bypass.

Background: Anterior inferior cerebellar artery (AICA) aneurysms are relatively rare in clinical practice, accounting for <1% of all intracranial arteries. After the diagnosis and location are confirmed by angiography, magnetic resonance, and other imaging examinations, interventional, or surgical treatment is often used, but some complex aneurysms require reconstructive surgery.Case Description: An 8-year-old male child was admitted to the hospital due to sudden disturbance of consciousness for 2 weeks. The head CT showed hematocele in the ventricular system with subarachnoid hemorrhage in the basilar cistern and annular cistern. On admission, he was conscious, answered correctly, had a soft neck, limb muscle strength was normal, and had no cranial nerves or nervous system abnormalities. A preoperative examination showed the right side of the anterior distal arteries class under the circular wide neck aneurysm, the distal anterior inferior cerebellar artery supplying a wide range of blood to the cerebellum, the ipsilateral posterior inferior cerebellar artery absent, and the aneurysm close to the VII, VIII nerves. The aneurysm was successfully treated by aneurysm resection and intracranial artery anastomosis in situ of a2 AICA-a2 AICA.Conclusions: AICA aneurysms are relatively rare; in this case, a complex wide-necked aneurysm was successfully treated by aneurysm resection and anastomosis in situ of a2 AICA-a2 AICA. This case can provide a reference for the surgical treatment of complex anterior cerebellar aneurysms.